The #NextflowSummit Barcelona lineup is finally here! 🥳 Meet some of our speakers: ➡️ Björn L. & Júlia Mir Pedrol, showcasing the latest nf-core advancements and its impact on bioinformatics communities. ➡️ Annick Renevey & Alexander Peltzer, discussing all things regulatory frameworks and clinical applications for nf-core pipelines. ⏳ This is just a sneak peek! Don’t wait—secure your ticket now and enjoy a 20% discount! 🎫🔥 Check out the full lineup of speakers here: https://lnkd.in/d3w_zQxm
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Introducing our HiFi-Somatic-WDL workflow for tumor-normal WGS variant analysis with PacBio HiFi reads! 🚀 We’ve optimized SNV, INDEL, SV, CNV, & DMR calling, plus you get an interactive report for quick analysis
Excited to launch our HiFi-Somatic-WDL workflow for tumor-normal WGS variant analysis with PacBio HiFi reads! 🚀 We benchmarked emerging tools and consolidated best practices for calling SNVs, INDELs, SVs, CNVs, & DMRs, plus an interactive report for quick analysis. Do reach out to us if you have any feedbacks as we seek to simplify bioinformatics for our customers! Link to workflow: https://lnkd.in/geV5mCVV
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An entity (person/machine) conducting life science research is called a Bioconductor ... update, upskill, connect. #biocverse #bioinformatics #r #biodatasci
📣 BioC2024: Registration Open Now ✨ Ready for the latest in bioinformatics? BioC2024 registration is live. Don’t miss your chance to join the conversation and expand your expertise. 🔗 Sign up here: https://buff.ly/3OQmuTs Got a knack for design? Enter our Sticker Design Contest to win your spot at the conference. 🖌️ Enter here: https://buff.ly/3PrejNR Join us to network, learn, and contribute to the Bioconductor community. #BioC2024 #Bioinformatics #RStats #BioconductorCommunity
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Hey #BiotechXEurope attendees! 🚀 Swing by booth #602 to chat with the DNAnexus team about the latest breakthroughs in bioinformatics software. Curious about how these innovations can transform your research? Drop by and let's discuss! https://hubs.ly/Q02RLTjR0 What are you most excited to learn about at the conference? #Bioinformatics #Innovation #DNAnexus
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Assoc Director, Global Software Product Marketing, Oncology, Genetic & Rare Disease Testing at Illumina
Bioinformatic analysis of large and complex multiomic datasets has become essential in the field of neuroscience. If you are attending #SfN24, connect with the Partek-Illumina team to see neuroscience informatics in action-- #DRAGEN for unmatched accuracy and comprehensiveness for variant calling and annotations and #Partek for variant insights and visualization. Learn how to power your discoveries at #SfN24 to see more! #Bioinformatics #Singlecell #RNASeq
We’ll be at #SfN24! Come see us at booth 630 to learn how Illumina bioinformatics software can make the most of your multiomic data. Ask us about demos and free trials. #Bioinformatics #Singlecell #RNASeq
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I'm happy to share that my research work, "Uncovering The Applicability of Machine Learning in Genomic Disease Prediction" has been published. It was mentioned in the 2nd International Conference on Disruptive Technologies (ICDT) proceedings of 2024. I sincerely thank Dr. Alpana and Dr. Mrinal Pandey for providing guidance and assistance during this journey. Also, I owe a special thanks to my co-author, Drishti Kemni, without whom this achievement would not have been possible. Do check it out! #ICDT2024 #research #machinelearning
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Join our 𝐅𝐑𝐄𝐄 webinar to explore the human body using bioinformatics in virtual reality, examine global policies and perspectives, and discover future capabilities with Andreas Bueckle, Ph.D. and Bruce Herr! 🧬 📆 Tuesday 28th May 2024 🕓 14:00 BST | 09:00 EDT 🖥️ Register here: https://hubs.la/Q02xxjqK0 𝐓𝐨𝐩𝐢𝐜𝐬 𝐢𝐧𝐜𝐥𝐮𝐝𝐞: ✔️ Exploring the human body using bioinformatics in virtual reality ✔️ Different global policies & perspectives ✔️ Future Capabilities #OGOmics #VirtualReality #Bioinformatics
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Get ready to decode the blueprint of life! bioinfoquant.com is launching soon. Stay tuned for powerful tools and insights at the intersection of bioinformatics and healthcare innovation. #bioinformatics
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Imagine saving a week or more on getting your libraries into your Lab. With Twist's new Library Design Tool you can say goodbye to the days of tedious DNA library design tasks and hello to a streamlined and efficient process so you can start your research sooner. Learn more here: https://lnkd.in/gzZjJMEb Twist Bioscience, #DNA, #librarydesign
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Illumina Complete Long Reads with Enrichment is now launched! This product has the ability to apply high-accuracy long reads to the human #genome to resolve challenging regions or add phased data over target regions. In addition to being flexible with low input and non-pristine DNA input--it's also compatible with a wide array of region and panel sizes. DM me for details or speak to my colleagues at #AGBT2024 and see our poster #594 by Stephen Bruinsma! #longread #genomesequencing
In 2023, we launched a novel technology to help reach the darkest corners of the genome and make long-read sequencing accessible. Now, we have built upon Illumina Complete Long Read technology with a new highly accurate, targeted long-read solution—compatible with predesigned and fully custom panels—offering greater flexibility for long-read sequencing. Why? To help scientists access more of the genome and find answers to improve human health. Learn more about Illumina Complete Long Read Prep with Enrichment: https://bit.ly/3Oliav7
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enabling digital services for Student Loan related activities while maintaining the highest security standard, the most compliant personal data protection and customer-centric data-driven innovation.
Exciting news in genomics data compression! We've just published a new blog post on arXiv (2404.02163v1) introducing FastqZip, an enhanced reference-based compression framework for FASTQ format files. Our work showcases FastqZip's ability to achieve a higher compression ratio than state-of-the-art algorithms, enabling more efficient storage and archiving of next-generation sequencing data. Learn more about this innovative approach: https://bit.ly/4aDr0NB
